Altered Epithelial-Mesenchymal Progenitor States Lead to Matrix Deposition, Tissue Inflammation, and Transitional Epithelial State in Congenital Diaphragmatic Hernia
CDH lung mesenchymal progenitors attain mesenchymal-like characteristics prematurely and there is upregulation of ECM proteins when compared to normal lung. Moreover, CDH distal epithelial cells (Krt8/18+) enter a transitional state that is seen in fibrotic lung diseases. These findings represent imbalance of EMT, and thus dysregulation of key molecular pathways, which leads to poorly developed mesenchymal and epithelial structures that we speculate causes the lung hypoplasia found in CDH.
Authors
- Micha Sam Brickman Raredon (ORCID: https://orcid.org/0000-0003-1441-6122)
- Mark Saltzman
- David H. Stitelman (ORCID: https://orcid.org/0000-0001-8067-5830)
- Satoshi Mizoguchi (ORCID: https://orcid.org/0000-0002-6099-1702)
- N.-K. Wang (ORCID: https://orcid.org/0009-0007-2670-7273)
- Rachel Rivero
- Sophie Edelstein (ORCID: https://orcid.org/0000-0003-0486-3244)
- Connor V Haynes (ORCID: https://orcid.org/0000-0001-6772-6365)
Institutions
- Yale University (US)
Publication Details
- Journal
- Fetal and Pediatric Pathology
- Published
- 2025-11-02
- DOI
- https://doi.org/10.1080/15513815.2025.2585371
- Primary Topic
- Congenital Diaphragmatic Hernia Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00